Phenotypes for disease #03876 (FANCQ (Fanconi anemia, complementation group Q (FANCQ)), OMIM:615272)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000017781 bilateral absent thumbs, microsomy, esophageal atresia, a ventrally translocated anus, dysplastic and low-set ears; Nodermatological abnormality such as skin hyperpigmentation, photosensitivity, sunlight-induced scarring, or atrophy; BMF at the age of 2 years - - Unknown - - - - - Arleen D. Auerbach 00020018
0000017782 such as perinatal growth retardation, short stature, pronounced microcephaly, cafe„-au-lait spots, an ostium-primum defect, biliary atresia with fibrosis of the liver, BMF;no spontaneous or UV-light-induced skin lesions - - Unknown - - - - - Arleen D. Auerbach 00020019
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.